Variant report
| Variant | rs73962065 |
|---|---|
| Chromosome Location | chr2:145433693-145433694 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:145423000-145440600 | Weak transcription | Primary hematopoietic stem cells | blood |
| 2 | chr2:145431400-145435400 | Weak transcription | Fetal Kidney | kidney |
| 3 | chr2:145432800-145434000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr2:145432800-145434200 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 5 | chr2:145432800-145435400 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
| 6 | chr2:145433000-145434000 | Enhancers | HMEC | breast |
| 7 | chr2:145433000-145434400 | Enhancers | NHEK | skin |
| 8 | chr2:145433000-145435400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 9 | chr2:145433000-145438800 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 10 | chr2:145433400-145434200 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
